Canonical Allele Identifier: CA891805153

Gene: SOAT1

Linked Data

• dbSNP Id: rs1222311855
• gnomAD v3: 1-179354499-G-A
• gnomAD v4: 1-179354499-G-A
• MyVariant Identifiers: chr1:g.179323634G>A (hg19) ; chr1:g.179354499G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.179354499G>A , CM000663.2:g.179354499G>A	GRCh38
NC_000001.10:g.179323634G>A , CM000663.1:g.179323634G>A	GRCh37
NC_000001.9:g.177590257G>A	NCBI36
NG_030638.1:g.65786G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000367619.8:c.*858G>A MANE Select	ENSP00000356591.3:n.*858G>A
ENST00000367619.7:c.*858G>A	ENSP00000356591.3:n.*858G>A
ENST00000539888.5:c.*858G>A	ENSP00000441356.1:n.*858G>A
ENST00000540564.5:c.*858G>A	ENSP00000445315.1:n.*858G>A
NM_001252511.1:c.*858G>A	NP_001239440.1:n.*858G>A
NM_001252512.1:c.*858G>A	NP_001239441.1:n.*858G>A
NM_003101.5:c.*858G>A	NP_003092.4:n.*858G>A
NR_045530.1:n.2661G>A
XM_011509911.1:c.*858G>A	XP_011508213.1:n.*858G>A
NM_003101.6:c.*858G>A MANE Select	NP_003092.4:n.*858G>A
NR_045530.2:n.2578G>A
NM_001252511.2:c.*858G>A	NP_001239440.1:n.*858G>A
NM_001252512.2:c.*858G>A	NP_001239441.1:n.*858G>A